Deep phenotyping of the Cdhr1-/- mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degeneration. (2021)
Attributed to:
Development of AAV gene therapy for blindness caused by cone-rod dystrophy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.exer.2021.108603
PubMed Identifier: 33964272
Publication URI: http://europepmc.org/abstract/MED/33964272
Type: Journal Article/Review
Volume: 208
Parent Publication: Experimental eye research
ISSN: 0014-4835